Melpida: Recombinant Adeno-associated Virus (Serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt)

Recruiting Phase 1 Phase 2 Interventional Study
Spasticity, Muscle Microcephaly Intellectual Deficiency Growth Retardation SPG50 Spastic Paraplegia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
4 Months – 10
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
4 (estimated)
Sponsor
Elpida Therapeutics SPC · Industry
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About This Trial
MELPIDA is proposed for the treatment of subjects with SPG50 and targets neuronal cells to deliver a fully functional human AP4M1 cDNA copy via intrathecal injection to counter the associated neuronal loss. Outcomes will evaluate the safety and tolerability of a single dose of MELPIDA, which will be measured by the treatment-associated adverse events (AEs) and serious adverse events (SAEs). Second…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age 4 months-10 years old 2. Confirmed diagnosis of SPG50 disease by: 1. Genomic DNA mutation analysis demonstrating homozygous or compound heterozygous, confirmed pathogenic variants in the AP4M1 gene 2. Clinical history or examination features consistent with SPG50 a…
Contacts

Elaine Most, MS

214-456-2463

elaine.most@utsouthwestern.edu

CONTACT